Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The aim of the study is to show that transplantation of lungs from Hepatitis B-infected donors is safe when using EVLP with UV light inactivation plus antivirals
The success of transplantation is significantly hindered by the lack of sufficient available donors. Many potential donor organs are not fully utilized in clinical transplantation because donors have chronic viral infections. Currently, donors with chronic hepatitis B virus (HBV) infection are utilized by typically providing nucleoside analogues such as entecavir or lamivudine plus/minus several doses of HBIG. The entecavir or lamivudine are typically given either life-long in liver transplants or for 1 year in non-liver transplants. Donors with chronic HBV infection are Core Antibody positive (HBcAb +ve). These donors carry chronic virus but may be NAT positive or NAT negative. HBcAb+ve donors are routinely used, but NAT positive donors are typically not used. The Toronto lung transplant program commonly applies Ex Vivo Lung Perfusion (EVLP) to organs. This allows for treatment of organs prior to transplantation. The investigators have shown that UV light administered on the EVLP circuit can substantially decrease the amount of infectious virus. Such a strategy was previously employed with hepatitis C virus. The aim of the study is to show that transplantation of organs from HBV NAT+ve donors is safe with the use of UV light treatment on EVLP combined with post-transplant antivirals for the recipient (HBIG and entecavir). The investigators hypothesize that rates of HBV transmission to recipients will be prevented by the use of this approach and any HBV transmission that does occur will be readily treatable. This will be a small pilot study to determine the feasibility of this approach. If successful, the knowledge from this study can have an important impact on patients awaiting lung transplantation by providing a novel strategy for the use of HBV-positive organ donors, simplified through a shorter course of approved antivirals.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| UV Light + Short-course Entecavir/HBIG | Experimental | Patients will receive lungs from HBV NAT+ donors, which will be treated with UV light therapy during ex-vivo perfusion. Patients will also receive Entecavir and HBIG prophylaxis in the immediate peri-operative period. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Entecavir | Drug | Recipients will receive 1mg administered orally, beginning pre-transplant as soon as the patient arrives to the hospital for surgery, and then 1mg post-operatively administered orally or via nasogastric tube once daily for 28 days. |
| Measure | Description | Time Frame |
|---|---|---|
| Safety of transplantation using HBV positive donors reflected by negative HBV NAT at 6 months post-transplant | Participant blood samples will be taken at days 3 and 7, then weekly for the first 4 weeks, then every two weeks until 12 weeks post-transplant, then at month 6 after transplantation. Blood samples will be tested for HBV DNA via Nucleic Acid Amplification. | At 6 months post-transplant |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of any HBV donor to recipient transmission | From enrollment until 2 years post-transplant | |
| Correlation between donor viremia level, and recipient infection | From enrollment until up to 2 years post-transplant |
Not provided
Donor Inclusion Criteria
Donor Exclusion Criteria
Recipient inclusion Criteria:
Recipient exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Atul Humar, MD, FRCPC | Contact | 416-340-4241 | atul.humar@uhn.ca |
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Health Network, Toronto General Hospital | Recruiting | Toronto | Ontario | M5G 2C4 | Canada |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D006509 | Hepatitis B |
| ID | Term |
|---|---|
| D000086982 | Blood-Borne Infections |
| D003141 | Communicable Diseases |
| D007239 | Infections |
| D018347 | Hepadnaviridae Infections |
Not provided
Not provided
| ID | Term |
|---|---|
| C413685 | entecavir |
| C045213 | hepatitis B hyperimmune globulin |
Not provided
Not provided
Not provided
The antiviral used are both approved drugs (entecavir and HBIG) but being used for a new indication
Not provided
Not provided
Not provided
Not provided
| HBIG | Biological | Recipients will receive 4500 IU intravenously pre-transplant and then at day 3 and 7 post-transplant (3 doses total). |
|
| EVLP UV Light Treatment | Device | UV light therapy will be administered to the organ during EVLP prior to transplantation. For minimum 2 hours, maximum 6 hours (duration determined by time clinically required for EVLP based on standard clinical assessment of lung). |
|
| Interval of time from transplantation to viremia development | From enrollment until 2 years post-transplant |
| HBV suppression rates after treatment for infected patients | From time of infection until end of treatment or up to 2 years post-transplant |
| Adverse reactions to antiviral therapy | From enrollment until 2 years post-transplant |
| Incidence of acute liver dysfunction for infected patients | From enrollment until 2 years post-transplant |
| In-hospital mortality | From hospital admission until date of discharge or date of death from any cause, whichever comes first, assessed up to 2 years |
| 1-year graft and patient survival | Measured 1 year post-transplant |
| Organ function at 1 year (FEV1) | Measured 1 year post-transplant |
| Development of anti-HBV antibodies (anti-HBs, anti-HBc) | From enrollment until 2 years post-transplant |
| D004266 |
| DNA Virus Infections |
| D014777 | Virus Diseases |
| D006525 | Hepatitis, Viral, Human |
| D006505 | Hepatitis |
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |